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1w5y
From Proteopedia
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[[Image:1w5y.png|left|200px]] | [[Image:1w5y.png|left|200px]] | ||
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{{STRUCTURE_1w5y| PDB=1w5y | SCENE= }} | {{STRUCTURE_1w5y| PDB=1w5y | SCENE= }} | ||
===HIV-1 PROTEASE IN COMPLEX WITH FLUORO SUBSTITUTED DIOL-BASED C2-SYMMETRIC INHIBITOR=== | ===HIV-1 PROTEASE IN COMPLEX WITH FLUORO SUBSTITUTED DIOL-BASED C2-SYMMETRIC INHIBITOR=== | ||
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{{ABSTRACT_PUBMED_15560801}} | {{ABSTRACT_PUBMED_15560801}} | ||
==About this Structure== | ==About this Structure== | ||
| - | + | [[1w5y]] is a 2 chain structure of [[Virus protease]] with sequence from [http://en.wikipedia.org/wiki/Human_immunodeficiency_virus Human immunodeficiency virus]. Full crystallographic information is available from [http://oca.weizmann.ac.il/oca-bin/ocashort?id=1W5Y OCA]. | |
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| + | ==See Also== | ||
| + | *[[Virus protease|Virus protease]] | ||
==Reference== | ==Reference== | ||
| - | <ref group="xtra">PMID: | + | <ref group="xtra">PMID:015560801</ref><references group="xtra"/> |
[[Category: HIV-1 retropepsin]] | [[Category: HIV-1 retropepsin]] | ||
[[Category: Human immunodeficiency virus]] | [[Category: Human immunodeficiency virus]] | ||
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[[Category: Dimer]] | [[Category: Dimer]] | ||
[[Category: Hydrolase]] | [[Category: Hydrolase]] | ||
| + | [[Category: Hydrolase-hydrolase inhibitor complex]] | ||
| + | [[Category: Hydrolase/hydrolase inhibitor]] | ||
[[Category: Protein-inhibitor complex]] | [[Category: Protein-inhibitor complex]] | ||
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| - | ''Page seeded by [http://oca.weizmann.ac.il/oca OCA ] on Mon Feb 16 23:41:54 2009'' | ||
Revision as of 02:15, 26 July 2012
Contents |
HIV-1 PROTEASE IN COMPLEX WITH FLUORO SUBSTITUTED DIOL-BASED C2-SYMMETRIC INHIBITOR
Template:ABSTRACT PUBMED 15560801
About this Structure
1w5y is a 2 chain structure of Virus protease with sequence from Human immunodeficiency virus. Full crystallographic information is available from OCA.
See Also
Reference
- Lindberg J, Pyring D, Lowgren S, Rosenquist A, Zuccarello G, Kvarnstrom I, Zhang H, Vrang L, Classon B, Hallberg A, Samuelsson B, Unge T. Symmetric fluoro-substituted diol-based HIV protease inhibitors. Ortho-fluorinated and meta-fluorinated P1/P1'-benzyloxy side groups significantly improve the antiviral activity and preserve binding efficacy. Eur J Biochem. 2004 Nov;271(22):4594-602. PMID:15560801 doi:10.1111/j.1432-1033.2004.04431.x
Categories: HIV-1 retropepsin | Human immunodeficiency virus | Claesson, B. | Hallberg, A. | Kvarnstroem, I. | Lindberg, J. | Loewgren, S. | Pyring, D. | Rosenquist, A. | Samuelsson, B. | Unge, T. | Vrang, L. | Zhang, H. | Zuccarello, G. | Dimer | Hydrolase | Hydrolase-hydrolase inhibitor complex | Hydrolase/hydrolase inhibitor | Protein-inhibitor complex
